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Ftir 1600

Manufactured by PerkinElmer
Sourced in United States

The FTIR-1600 is a Fourier Transform Infrared (FTIR) spectrometer. It is capable of analyzing the infrared absorption spectrum of a sample. The FTIR-1600 uses an interferometer to generate and detect infrared light, which is then used to identify the chemical composition of the sample.

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7 protocols using ftir 1600

1

Structural Analysis of T-NPs via XRD

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The structural nature of the T-NPs was evaluated using XRD (Perkin-Elmer FTIR-1600, Massachusetts, USA). The samples were run between 20 and 70 2θ [28 (link)]. The particle size of T-NPs was also calculated, using the Debye-Scherrer equation given below.
Debye-Scherrer equation=τ=Kλβ cosθ
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2

FTIR Characterization of Nano Curcumin

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Nano curcu were characterized by FTIR (Perkin-Elmer FTIR-1600, USA) mixing dried powder of nanoparticles with KBr. Spectra were taken in the range of 500–2000 cm−1 at a resolution of 4 cm−1. The data of FTIR reveal information about functional groups which are present in the Nano curcu.
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3

Comprehensive Characterization of Biologically Synthesized Silver Nanoparticles

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AgNPs were characterized according to methods used by Saied et al. [34 (link)]. A reaction mix ranging from light yellow to brownish was formed after 24 h. The formation of AgNPs was thought to be indicated by this color change, in which the color shift of control was not seen as compared to the sample. The results were confirmed using conventional characterization methods, such as a UV–visible spectrophotometer (scanning spectra 109 range from 300 to 700 nm, Shimadzu UV-1700, Kyoto, Japan). The morphology of AgNPs was examined using transmission electron microscopy (JEOL 1010 TEM, Japan). The functional groups involved in reducing, capping, and stabilization of AgNPs were studied using Fourier transform infrared spectroscopy (FTIR) (Perkin-Elmer FTIR-1600, USA) by following the standard operating protocol, and the spectral bands of prepared (crystallized form) AgNPs were determined with 400–4000 cm−1. X-ray diffraction (XRD) (Shimadzu LabX XRD-6000) with a Cu-Kα X-ray source (λ = 1.5418 Å) analysis was used to evaluate the crystallite nature of AgNPs. The average particle size and size distribution of AgNPs in colloidal solutions were determined by dynamic light scattering (DLS) (The Nicomp ZLS Z 3000, USA).
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4

Characterization of Organic Compounds

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Melting points were determined with a Buchi Melting Point B-450. 1H and 13C-NMR spectra were recorded on a Varian Mercury 300 spectrometer. Proton chemical shifts were referred to the TMS internal standard. Chemical shifts are reported in parts per million (ppm, δ units). Coupling constants are reported in units of Hertz (Hz). Splitting patterns are designed as s, singlet; d, doublet; t, triplet; q quartet; qnt quintet; dd, double doublet; m, multiplet; b, broad. Infrared spectra were recorded on a FT-IR 1600 Perkin Elmer. All commercial chemicals and solvents are reagent grade and were used without further purification unless otherwise specified. All reactions were carried out with the use of the standard techniques and were monitored by thin-layer chromatography on silica gel plates (60F-254, E. Merck, Merck Group, Darmstadt, Germany) and visualized with UV light.
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5

Characterization of Multifunctional Polymer Gel

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The structure of the polymer was confirmed by Bruker NMR spectrometer (using deuterated DMSO as the solvent). The chemical groups of the composite are characterized by fourier transform infrared spectroscopy (FTIR, PerkinElmer model 1600-FTIR). The rheological properties of the gel were determined by a rheometer (Discovery Hybrid Rheometer (HR2), TA instruments.). The sol-gel transition of the PDNPs-PELA solution is demonstrated by flip test. The morphology of PDNPs in the gel was characterized by FEI Tecnai F20 transmission electron microscope. Photoacoustic imaging was captured using the Vevo LAZR photoacoustic-micro-ultrasound imaging system (FUJIFILM VisualSonics, Toronto, Canada) with a 21 MHz center frequency probe. The particle size was measured using DLS (Malvern, Zetasizer Nano ZS90).
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6

Characterization of Novel Thiazolidinone Compounds

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Melting points were determined in open capillary tubes with a Buchi B-540 melting point apparatus and are uncorrected. Microanalyses were performed on a Thermo Finnigan Flash EA 1112 elemental analyzer. IR spectra were recorded in KBr discs (νmax in cm−1) on a Perkin–Elmer 1600 FTIR. 1H NMR (DMSO-d6),13C NMR (Proton decoupled, APT) (DMSO-d6) and heteronuclearcorrelation 1H–13C (HSQC, HMBC) (DMSO-d6) spectra were run on Bruker AC 200 (200 MHz) and VarianUNITYINOVA (500 MHz) instruments. Chemical shifts are reported as δ (ppm) relative to TMS as internal standard and coupling constants (J) are given in Hertz (Hz). MS (ESI−) were determined on a Finnigan LCQ Advantage Max mass spectrometer (br: broad, ind.: indole, thz.: thiazolidinone).
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7

Characterization of Hydrogel Formulations

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Fourier Transform Infrared Spectroscopy (FTIR) was used to indicate specific chemical groups in the formulation and materials 4, 5 . The infrared spectrum studies of hydrogels were performed (Perkin Elmer 1600 FT-IR, England). Before starting the study, hydrogels were converted into lyophilized powder with a lyophilizer. Infrared spectrum measurements of chitosan, PVA, rh-EGF and mPEG propionaldehyde were performed with the same method.
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